Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes)

Development Growth and Differentiation

Volumn 54, Issue 5, 2012, Pages 588-604

  Morita, Akihiro ^a,e   Nakahira, Kumiko ^a   Hasegawa, Taeko ^a   Uchida, Kaoru ^a   Taniguchi, Yoshihito ^b,f   Takeda, Shunichi ^b   Toyoda, Atsushi ^c,g   Sakaki, Yoshiyuki ^c,h   Shimada, Atsuko ^d   Takeda, Hiroyuki ^d   Yanagihara, Itaru ^a  

^a RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c RIKEN YOKOHAMA INSTITUTE   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

^e SUZUKA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

^f KEIO UNIVERSITY   (Japan)

^g NATIONAL INSTITUTE OF GENETICS   (Japan)

^h TOYOHASHI UNIVERSITY OF TECHNOLOGY   (Japan)

Author keywords

ESCO2; Oryzias latipes; Premature chromosomal separation; Roberts syndrome and SC phocomelia

Indexed keywords

COMPLEMENTARY DNA; NOTCH1 RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; DOWN REGULATION; EMBRYO; EMBRYO DEATH; ESCO2 GENE; GENE; GENE EXPRESSION; GENE LIBRARY; GENE MUTATION; GENETIC ANALYSIS; GENETIC CONSERVATION; GENETIC MODEL; GENETIC SCREENING; HOMOZYGOSITY; MOLECULAR CLONING; NONHUMAN; ORYZIAS; PHOCOMELIA; ROBERTS SYNDROME; TARGETING INDUCED LOCAL LESIONS IN GENOMES METHOD;

ACETYLTRANSFERASES; ANIMALS; APOPTOSIS; CLONING, MOLECULAR; CRANIOFACIAL ABNORMALITIES; DISEASE MODELS, ANIMAL; ECTROMELIA; GENOTYPE; HYPERTELORISM; ORYZIAS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTOR, NOTCH1; REVERSE GENETICS;

EID: 84862690412     PISSN: 00121592     EISSN: 1440169X     Source Type: Journal    
DOI: 10.1111/j.1440-169X.2012.01362.x     Document Type: Article

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